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GRCh37/hg19 8p21.2(chr8:24157516-24483615)x3 AND See cases

Significance: Uncertain significance
ClinVar: RCV000446073

Variant: GRCh37/hg19 8p21.2(chr8:24157516-24483615)x3

Type: Variant
Allele: GRCh37/hg19 8p21.2(chr8:24157516-24483615)x3 382357
Gene:
Type: copy number gain
Location: Chr8: 24157516 - 24483615 - assembly GRCh37
References: dbVar: nsv2778027
dbVar: nssv13649472

Condition

PhenotypeInstruction: See cases